EP1119591B1 - Concentrated stripper composition and method - Google Patents

Concentrated stripper composition and method Download PDF

Info

Publication number
EP1119591B1
EP1119591B1 EP99954639A EP99954639A EP1119591B1 EP 1119591 B1 EP1119591 B1 EP 1119591B1 EP 99954639 A EP99954639 A EP 99954639A EP 99954639 A EP99954639 A EP 99954639A EP 1119591 B1 EP1119591 B1 EP 1119591B1
Authority
EP
European Patent Office
Prior art keywords
composition
water
accordance
solvent mixture
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP99954639A
Other languages
German (de)
French (fr)
Other versions
EP1119591A1 (en
Inventor
Paul M. Hernandez
Lance D. Brown
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Diversey Inc
Original Assignee
JohnsonDiversey Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JohnsonDiversey Inc filed Critical JohnsonDiversey Inc
Publication of EP1119591A1 publication Critical patent/EP1119591A1/en
Application granted granted Critical
Publication of EP1119591B1 publication Critical patent/EP1119591B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D9/00Chemical paint or ink removers
    • C09D9/005Chemical paint or ink removers containing organic solvents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/43Solvents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/05Alcohols; Metal alcoholates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/06Ethers; Acetals; Ketals; Ortho-esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/17Amines; Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D9/00Chemical paint or ink removers
    • C09D9/04Chemical paint or ink removers with surface-active agents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/06Ether- or thioether carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/044Hydroxides or bases
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2034Monohydric alcohols aromatic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2068Ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/30Amines; Substituted amines ; Quaternized amines

Definitions

  • This invention relates to compositions and methods of using compositions to strip or remove coatings such as typical floor finishes and cleaning of such surfaces. More particularly, it relates to a stripping composition which can be diluted and still provide efficient stripping.
  • U.S. Patent 5,637,559 from 3M discloses a floor stripping composition which includes a phenyl substituted alkyl alcohol which preferably is benzyl alcohol having a water solubility of at least 0.1 weight percent, a coupler consisting of a fatty acid of C8 in chain length and water. The coupler is at least 3.0 times the amount necessary to completely solubilize the phenyl substituted alkyl alcohol in the water.
  • Preferred couplers are the salt of a monofunctional water-soluble amine and an organic acid comprising at least one water-insoluble organic acid having from 6-10 carbon atoms.
  • Patents 5,080,831; 5,080,822 and 5,158,710 from Buckeye International, Inc. teach the use of sparingly water soluble solvents when used with a hydrotrope to form a aqueous solution or microemulsion that can used as a stripper.
  • the solvents, such as benzyl alcohol, cited in these patents have a water solubility ranging from 0.2 to approximately 6 weight percent in water.
  • the solubilizing agent is present in an amount not exceeding approximately twofold that required to completely solubilize the organic solvent.
  • Japanese Patent JP 9689885 assigned to S.C. Johnson Inc.
  • Benzyl alcohol is also disclosed with Tall Oil Fatty Acid as the organic acid which when combined with a monofunctional water-soluble amine as the coupler form an aqueous floor finish stripper.
  • compositions containing at least two specific solvents from the select class of slightly water-soluble organic solvents and a specific coupler, wherein the coupler is present at greater than 2.0 times that required to completely solubilize the solvent are much more efficient in removing a variety of floor finishes at higher dilutions than prior art compositions.
  • the other unique property of the inventive composition is the ability to remove these floor finishes of higher dilutions than the prior art compositions and the ability to remain stable in the concentrate as well as in dilution.
  • Another surprising attribute that has been uncovered is the ability of these compositions to be diluted in hard water and still being stable and effacaeous.
  • compositions of this invention which are suitable for stripping of various floor finish coatings, such as acrylic, urethane and epoxy polymer base, from a variety of surfaces, such as vinyl composition, terrazzo, marble, linoleum, concrete and the like as well as an effective cleaner/degreaser after being diluted with water from 1 part of said compositions to 50 parts of water and still remove the finish.
  • the compositions may be formulated comprising:
  • the water-soluble organic amine is monoethanolamine or a combination of monoethanolamine and potassium hydroxide.
  • the acid is a C9-C11 ethoxylated anionic surfactant and has 4 moles of ethoxylation.
  • the phenyl substituted alkyl alcohol is benzyl alcohol
  • the alkyl glycol ether is ethylene glycol monohexyl ether.
  • the coupler includes tall oil.
  • Disposed with water means the inventive compositions are reduced in actives concentration by adding from 0.1 part of 100 parts of water per part of inventive composition. Specific dilution ratio are dependent on the end use, as shown in the following Examples. Additionally the water hardness described is from 0 ppm to 450 ppm hardness as CaCO 3 .
  • Effective amount when referring to the solvent blend of phenyl substituted alkyl alcohol and alkyl glycol ether means that is present in an amount which removes at least 20 percent of a standard urethane/acrylic floor finish from a composition vinyl tile within fewer than 2.5 minutes, in accordance with a standard test (see Test Methods section).
  • the term "coupler” refers to a compound or a physical or chemical combination of compounds having the capability of increasing the phase-stability of the compositions of the invention.
  • the couplers that are preferred comprise low molecular weight (molecular weights in the 300 to 800 range) organic monoethanolamine and alkaline salts either sodium hydroxide or potassium hydroxide with organic acid (tall oil) and ethoxylated carboxylic acid (C9-C11 carboxylic acid with 4 moles of ethoxylation; trade name of Neodox 1-4).
  • compositions can also include an effective amount of chelating agents (e.g. ethylene diaminietriacetic acid) and other surfactants for added stability and enhanced hard water stability but are not crucial to this invention.
  • chelating agents e.g. ethylene diaminietriacetic acid
  • Water soluble solvents such as ethylene glycol monobutyl ether can also be used with this invention to enhance cleaning and stripping ability.
  • compositions of the invention are substantially more effective in removing multiple/difficult to remove floor sealer/finishes comprising of urethane/acrylic polymers than the previously described patented compositions, as shown in the Examples.
  • Another aspect of the invention is a method of removing a sealer/finish coating from a surface, the method comprising:
  • Preferred methods comprise of abrading the coating after a predetermined contact time between the coating and the composition, such as with an open three dimensional non-woven pad which is attached to a conventional floor maintenance machine.
  • composition may be applied and removed using other natural and synthetic fiber-based cloth.
  • compositions of the present invention are especially useful in stripping a variety of difficult to strip "sealer/finishes" from flooring materials such as composition vinyl tiles, linoleum, marble, terrazzo, concrete and the like.
  • the compositions of the invention may also be employed in degreasing grease, oil, cooking oils and the like from a variety of floors in restaurants, homes, automobile shops and the like.
  • the compositions of the invention may also be employed in cleaning a variety of other surfaces other than floors.
  • the various ingredients are discussed in more detail.
  • Phenyl substituted alkyl alcohols are the first solvents and function as the coating dissolver and/or grease solubilizing component of the compositions of the invention.
  • the phenyl substituted alkyl alcohols are from the class of "sparingly” or “slightly” water soluble organic solvents which have water solubility of at least 0.1 weight percent, more preferable ranging from about 0.2 to about 6 weight percent.
  • Phenyl substituted alkyl alcohols useful in the invention include benzyl alcohol, alpha-phenylethyl alcohol, betaphenylethyl alcohol, ethylene glycol phenyl ether, and the like.
  • One of the preferred phenyl substituted alkyl alcohols which is slightly water-soluble is benzyl alcohol.
  • the second solvent used in the invention is from the alkyl glycol ether family and it functions in that it increases the wetting as well as the dissolving ability of the benzyl alcohol.
  • the preferred secondary solvent is ethylene glycol hexyl ether (Trade name Hexyl Cellosolve) and it too is a "sparing soluble" solvent with similar properties of low toxicity, availability, relative nonhazardous to transport with a essentially a non-odor as benzyl alcohol.
  • alkyl as used herein means an alkyl group having 1-10 carbon atoms.
  • the phenyl substituted alkyl alcohols and the alkyl glycol ether employed in the invention have a relatively low volatility or high flash point (in excess of 60 C.) exhibit a low level of odor, be chemically stable, non-toxic, nonhazardous and commercially available.
  • compositions within the invention preferably have the following weight ratios of active ingredients:
  • the weight percentage of phenyl substituted alkyl alcohols/alkyl glycol ethers in the ready-to-use composition may be as high as 10 weight percent.
  • a preferred ready-to-use composition includes from 1.0 to 3.5 wt % of solvent. These concentrations of solvent combinations may be diluted as the concentrates listed in Table 1. For cleaning compositions the solvent mixture will have the power to remove greasy residues at less than 1 weight percent.
  • Concentrate 1 Concentrate 2
  • Couplers function to increase the phase stability of the composition by increasing the apparent water solubility of the solvent mix.
  • Suitable couplers for use in the compositions of the present invention include the salt of a low molecular weight monofunctional amine as well as alkaline salts such as sodium hydroxide and potassium hydroxide as well as organic acid. These couplers allow the use of high concentration of solvent coupled/emulsified and are instrumental in the stability of the product as well as stability of the diluted product.
  • Particularly preferred monofunctional amines include water soluble organic amines such as monoethanolamine (MEA), 2-aminomethylprpanol (AMPS), and other n-alkyl substituted derivatives of these.
  • Preferred acids include fatty acids (tall oil) as well as C7-C18 carboxylic acids with ethoxylation of 1-10 moles of ethylene oxide.
  • tall oil and the carboxylate Neodox 1-4 available from Shell Chemical Co. is especially preferred.
  • ethoxylated organic acid that it not only improves product stability but enhances the stability of the concentrate when diluted in hard water so that no additional builder or chelate is necessary.
  • alkaline salts like sodium hydroxide and potassium hydroxide.
  • couplers are present in ready-to-use compositions of the invention such that the amount of the coupler is always less than or equal to the solvent blend used. This a departure from previous taught patents where said coupler are either equal to or as much as 3.0 times necessary to solubilize the solvents in water.
  • Tergitols such as Tergitol 15-S-9, which has been found to be useful in making formulations not containing ethoxylated carboxylates, however they are not the preferred surfactants.
  • Tergitol is a trademark of Union Carbide Corporation for C8-C18 nonionic surfactants with 1-15 moles of ethylene oxide.
  • anionic surfactants that have found utility are the well known hydrotropes like sodium xylene sulfonate as well as the following: dodecylbenzene sulfonic acid, sodium dodecylbenzene sulfonate, potassium dodecylbenzene sulfonate, triethanolamine dodecylbenzene sulfonate, morpholinium dodecylbenzene sulfonate, ammonium dodecylbenzene sulfonate, isopropylamine dodecylbenzene sulfonate, sodium tridecylbenzene sulfonate, sodium dinonylbenzene sulfonate, potassium didodecylbenzene sulfonate, dodecyl diphenyloxide disulfonic acid, sodium dodecyl diphenyloxide disulfonate, isopropylamine decyl dipheny
  • compositions can also be thickened and used for various other applications especially for vertical surfaces and as an aerosol applications.
  • Prior art describes the use of specific ingredients that are useful for those applications.
  • compositions of the invention may be applied with a mop, poured onto the surface to be cleaned or stripped as well as dispensed from a suitable dispenser such as one of the venturi type (J-Fill dispenser).
  • a suitable dispenser such as one of the venturi type (J-Fill dispenser).
  • the compositions may also be applied by conventional floor maintenance machines, or they may be sprayed as an aerosol or non-aerosol upon the surface to be cleaned. Spraying can be accomplished by conventional mechanical spraying devices or by using an aerosol dispensing container with a sufficient amount of suitable aerosol propellant, for example, low boiling alkanes or mixtures thereof, such as a mixture of isobutane and propane..
  • compositions and methods of the invention will be understood with reference to the following Examples wherein all parts and percentages are by weight unless otherwise specified. These Examples are set forth to illustrate the invention and are not intended to limit the invention in any way.
  • compositions shown in Table 1 above were diluted with water at the dilutions indicated in Table 2 to formulate the compositions of Examples 1-2.
  • Table 2 also shows additional formulations and the various key compositions tested to arrive at the compositions of this invention.
  • the compositions of comparative Examples A-C in Table 3 were formulated in accordance with the teaching of U.S. Patent No. 5,158,710; U.S. Patent No. 5,637,559 and Japanese Patent 9689885 and are provided in prior art Examples A-C.
  • Example 1-7 and Comparative Examples A-C were tested to determine their proficiency in removing 10 coats of a commercially available acrylic finishes from a composition vinyl tile strip, the finish available from SC Johnson Professional, Racine, WI under the trade designation of Signature. To clean previously stripped tiles 10 coats of finish was applied. After each coat a crayon marker was used to identify each coat. The Signature coated tiles were burnished (high speed burnisher) after 3, 6 and 10th coat prior to oven aging in order to enhance and duplicate actual aged coatings found in commerce. After all 10 coats were applied the tiles were aged in a oven at 52°C (125 F)for 100 hours to allow the coating to fully harden and thus simulate aged coating.
  • compositions of Examples 1-7 as well as Comparative Examples A-C were then tested via the use of a Gardner Scrubber by placing strips of tiles treated and identified onto the bed of the Scrubber. Each strip of tile was stripped with a red non-woven nylon pad which was attached to a pulley and is dragged over the tile to simulate the type of abrasion done in actual practice. To each strip of tile 15 mls of diluted concentrated stripper solutions were applied to the tile. Immediately after the solution was applied the Gardner Scrubber was started and number of coats removed versus cycles was recorded. In all Examples, the number of maximum cycles used was 100 cycles or less depending on complete removal.
  • composition stability was to make up the composition and subject it to both 4°C (40 F) and 52°C (125 F) in a refrigerator or oven for at least 3 days The results are also included.
  • a second test which determined the stability of the diluted product was done by diluting the concentrates in synthetic 300 ppm hard water (as CaCO3). The results from this test is also indicated in the Tables. These tests are used by those skilled in the art of developing compositions and are readily accepted as an indication of the overall microemulsion properties and efficiency of the surfactants/solvents used.
  • the third test run was viscosity at 7°C (44 F) which gives a good indication of the rheology of the composition and is crucial in dispensing from venturi type dispenser (J-Fill), The lower the viscosity the more accurate the dilutions which are critical in performance. Viscosities greater than 50 cps can be used but viscosities less than 40 cps are preferred.
  • alkyl and aryl ethers as well as alkyl alcohols have been indicated for use with the phenyl substituted alkyl alcohols of this invention, other alkyl and aryl ethers as well as alkyl and aromatic alcohols can be employed which are described as follows according to their water solubility.
  • compositions of this invention are useful in stripping and removing coatings such as floor finishes as well as the cleaning of such surfaces. They can be diluted with water and still provide stripping and cleaning properties.

Abstract

The present invention is directed to a composition for stripping coatings from a surface, the composition including: a. A solvent mixture composed of a phenyl substituted alkyl alcohol and an alkyl or aryl glycol ether or an alkyl or aromatic alcohol; b. A coupler composed of a salt formed from a water soluble organic amine and an acid comprising at least one C7-C18 ethoxylated anionic surfactant; c. Optionally water. The use of the C7-C18 ethoxylated anionic surfactant provides a stripper which can be diluted in water of various compositions yet provide an effective stripping/cleaning agent.

Description

BACKGROUND OF THE INVENTION Technical Field
This invention relates to compositions and methods of using compositions to strip or remove coatings such as typical floor finishes and cleaning of such surfaces. More particularly, it relates to a stripping composition which can be diluted and still provide efficient stripping.
Background Art
There are available numerous concentrated stripper and cleaner/degreaser formulations for use in conjunction with floors. U.S. Patent 5,637,559 from 3M discloses a floor stripping composition which includes a phenyl substituted alkyl alcohol which preferably is benzyl alcohol having a water solubility of at least 0.1 weight percent, a coupler consisting of a fatty acid of C8 in chain length and water. The coupler is at least 3.0 times the amount necessary to completely solubilize the phenyl substituted alkyl alcohol in the water. Preferred couplers are the salt of a monofunctional water-soluble amine and an organic acid comprising at least one water-insoluble organic acid having from 6-10 carbon atoms. U.S. Patents 5,080,831; 5,080,822 and 5,158,710 from Buckeye International, Inc. teach the use of sparingly water soluble solvents when used with a hydrotrope to form a aqueous solution or microemulsion that can used as a stripper. The solvents, such as benzyl alcohol, cited in these patents have a water solubility ranging from 0.2 to approximately 6 weight percent in water. In the '831 Patent the solubilizing agent is present in an amount not exceeding approximately twofold that required to completely solubilize the organic solvent. Japanese Patent JP 9689885 assigned to S.C. Johnson Inc. teaches the use of a phenyl substituted alkyl alcohol having a water solubility of at least 0.1 weight percent. Benzyl alcohol is also disclosed with Tall Oil Fatty Acid as the organic acid which when combined with a monofunctional water-soluble amine as the coupler form an aqueous floor finish stripper.
Other cleaning compositions with a specific solvent or surface active agent are described in U.S. Patents 4,749,509 and 5,543,073.
SUMMARY OF THE INVENTION
Contrary to the teachings of the art, the inventors have discovered that compositions containing at least two specific solvents from the select class of slightly water-soluble organic solvents and a specific coupler, wherein the coupler is present at greater than 2.0 times that required to completely solubilize the solvent are much more efficient in removing a variety of floor finishes at higher dilutions than prior art compositions. The other unique property of the inventive composition is the ability to remove these floor finishes of higher dilutions than the prior art compositions and the ability to remain stable in the concentrate as well as in dilution. Another surprising attribute that has been uncovered is the ability of these compositions to be diluted in hard water and still being stable and effacaeous. The use of a new coupling agent has also given these compositions the ability to be prepared using alkaline salts such as NaOH and KOH and still be stable in the concentrate as well as in dilution which the prior art compositions are not. The use of a new coupler has also the added feature of being less viscous and therefore is easier to be diluted via dispensing equipment and other typical dilution methods.
The objects of the invention therefore are:
  • a. Providing an improved floor coating stripper composition.
  • b. Providing an improved stripper composition of the foregoing kind which is compatible with water of various compositions.
  • c. Providing an improved stripper composition of the foregoing kind which can be diluted in the 1:30-1:50 range and still be effective.
  • d. Providing an improved stripper of the foregoing kind which can be dispensed with automated dispensing systems.
  • The foregoing objects are accomplished and the shortcomings of the prior art are overcome by the compositions of this invention which are suitable for stripping of various floor finish coatings, such as acrylic, urethane and epoxy polymer base, from a variety of surfaces, such as vinyl composition, terrazzo, marble, linoleum, concrete and the like as well as an effective cleaner/degreaser after being diluted with water from 1 part of said compositions to 50 parts of water and still remove the finish. In one embodiment, the compositions may be formulated comprising:
  • a. About 1-55% by weight of a solvent mixture composed of a phenyl substituted alkyl alcohol and an equal amount of an alkyl or aryl glycol ether or an alkyl or aromatic alcohol, the solvent mixture effective in removing at least 20% of a standard acrylic floor sealer/finish from a composition vinyl tile in fewer than 2.5 minutes;
  • b. a coupler composed of a salt formed from a water soluble organic amine and an acid comprising at least one C7-C18 ethoxylated anionic surfactant, the coupler and the solvent mixture present in a weight ratio of about 1:1.2 to about 1:2.0 wherein the amount of the coupler is at least 2.0 times the amount necessary to completely solubilize the solvent mixture; and
  • c. optionally water.
  • In another embodiment, the water-soluble organic amine is monoethanolamine or a combination of monoethanolamine and potassium hydroxide.
    In yet another embodiment, the acid is a C9-C11 ethoxylated anionic surfactant and has 4 moles of ethoxylation.
    In still another embodiment, the phenyl substituted alkyl alcohol is benzyl alcohol, and the alkyl glycol ether is ethylene glycol monohexyl ether.
    In yet another embodiment, the coupler includes tall oil.
    "Diluted with water" as used herein means the inventive compositions are reduced in actives concentration by adding from 0.1 part of 100 parts of water per part of inventive composition. Specific dilution ratio are dependent on the end use, as shown in the following Examples. Additionally the water hardness described is from 0 ppm to 450 ppm hardness as CaCO3.
    "Effective amount" when referring to the solvent blend of phenyl substituted alkyl alcohol and alkyl glycol ether means that is present in an amount which removes at least 20 percent of a standard urethane/acrylic floor finish from a composition vinyl tile within fewer than 2.5 minutes, in accordance with a standard test (see Test Methods section).
    As used herein the term "coupler" refers to a compound or a physical or chemical combination of compounds having the capability of increasing the phase-stability of the compositions of the invention. The couplers that are preferred comprise low molecular weight (molecular weights in the 300 to 800 range) organic monoethanolamine and alkaline salts either sodium hydroxide or potassium hydroxide with organic acid (tall oil) and ethoxylated carboxylic acid (C9-C11 carboxylic acid with 4 moles of ethoxylation; trade name of Neodox 1-4).
    The compositions can also include an effective amount of chelating agents (e.g. ethylene diaminietriacetic acid) and other surfactants for added stability and enhanced hard water stability but are not crucial to this invention. Water soluble solvents such as ethylene glycol monobutyl ether can also be used with this invention to enhance cleaning and stripping ability.
    The compositions of the invention are substantially more effective in removing multiple/difficult to remove floor sealer/finishes comprising of urethane/acrylic polymers than the previously described patented compositions, as shown in the Examples.
    Another aspect of the invention is a method of removing a sealer/finish coating from a surface, the method comprising:
  • a. applying to the coating a composition within the invention; and
  • b. allowing the composition to contact the coating for a time sufficient to at least partially remove the coating. As used herein "coating" is meant to include a single layer or multiple layers of the same composition and coatings comprising two or more layers, each layer comprising of dissimilar compositions.
  • Preferred methods comprise of abrading the coating after a predetermined contact time between the coating and the composition, such as with an open three dimensional non-woven pad which is attached to a conventional floor maintenance machine.
    Alternatively, the composition may be applied and removed using other natural and synthetic fiber-based cloth.
    Further aspects and advantages of the invention will become apparent from the description of the preferred embodiments which follows.
    DESCRIPTION OF PREFERRED EMBODIMENTS
    The compositions of the present invention are especially useful in stripping a variety of difficult to strip "sealer/finishes" from flooring materials such as composition vinyl tiles, linoleum, marble, terrazzo, concrete and the like. The compositions of the invention may also be employed in degreasing grease, oil, cooking oils and the like from a variety of floors in restaurants, homes, automobile shops and the like. The compositions of the invention may also be employed in cleaning a variety of other surfaces other than floors. The various ingredients are discussed in more detail.
    Phenyl Substituted Alkyl Alcohols
    Phenyl substituted alkyl alcohols are the first solvents and function as the coating dissolver and/or grease solubilizing component of the compositions of the invention. The phenyl substituted alkyl alcohols are from the class of "sparingly" or "slightly" water soluble organic solvents which have water solubility of at least 0.1 weight percent, more preferable ranging from about 0.2 to about 6 weight percent. Phenyl substituted alkyl alcohols useful in the invention include benzyl alcohol, alpha-phenylethyl alcohol, betaphenylethyl alcohol, ethylene glycol phenyl ether, and the like. One of the preferred phenyl substituted alkyl alcohols which is slightly water-soluble is benzyl alcohol.
    The second solvent used in the invention is from the alkyl glycol ether family and it functions in that it increases the wetting as well as the dissolving ability of the benzyl alcohol. The preferred secondary solvent is ethylene glycol hexyl ether (Trade name Hexyl Cellosolve) and it too is a "sparing soluble" solvent with similar properties of low toxicity, availability, relative nonhazardous to transport with a essentially a non-odor as benzyl alcohol.
    The term "alkyl" as used herein means an alkyl group having 1-10 carbon atoms.
    In addition to the water solubility criteria mentioned previously, it is also desirable but not essential that the phenyl substituted alkyl alcohols and the alkyl glycol ether employed in the invention have a relatively low volatility or high flash point (in excess of 60 C.) exhibit a low level of odor, be chemically stable, non-toxic, nonhazardous and commercially available.
    We have found the use of phenyl substituted alkyl alcohol in conjunction with the use of alkyl or aryl glycol ether or an alkyl or aromatic alcohol in equal proportions in the composition as having unexpected results not found by the use of either one individually. This solvent mix is in an amount sufficient to remove the coating to which it is applied, the amount varying with the coating or residue to be removed. Further compositions within the invention preferably have the following weight ratios of active ingredients:
  • Phenyl substituted alkyl alcohol to coupler, from 1:1 to 1:2.0. Preferably 1:1.6.
  • Alkyl glycol ether to coupler, from 1:1 to 1:2.0. Preferably 1:16.
  • Phenyl substituted alkyl alcohol to anionic surfactant from 1:10. Preferably 1:1.5.
  • Alkyl glycol ether to anionic surfactant from 1:10. Preferably 1:5.5.
  • For particularly hard to remove coatings the weight percentage of phenyl substituted alkyl alcohols/alkyl glycol ethers in the ready-to-use composition may be as high as 10 weight percent. For easier to strip finishes or cleaning, one may dilute the concentrates so that the weight percentage of phenyl substituted alkyl alcohols/alkyl glycol ethers is as low as 0.5 weight percent. A preferred ready-to-use composition includes from 1.0 to 3.5 wt % of solvent. These concentrations of solvent combinations may be diluted as the concentrates listed in Table 1. For cleaning compositions the solvent mixture will have the power to remove greasy residues at less than 1 weight percent.
    The following Table 1 illustrates two of the preferred compositions of this invention.
    Concentrate 1 Concentrate 2
    Ingredient
    Benzyl alcohol 27.5 27.5
    Hexyl Cellosolve 27.5 27.5
    Monoethanolamine 35.0 17.0
    Tall Oil Fatty acid 5.0
    Neodox 1-4 5.0 10.0
    Potassium hydroxide -- 18.0
    Couplers
    Couplers function to increase the phase stability of the composition by increasing the apparent water solubility of the solvent mix. Suitable couplers for use in the compositions of the present invention include the salt of a low molecular weight monofunctional amine as well as alkaline salts such as sodium hydroxide and potassium hydroxide as well as organic acid. These couplers allow the use of high concentration of solvent coupled/emulsified and are instrumental in the stability of the product as well as stability of the diluted product. Particularly preferred monofunctional amines include water soluble organic amines such as monoethanolamine (MEA), 2-aminomethylprpanol (AMPS), and other n-alkyl substituted derivatives of these.
    Preferred acids include fatty acids (tall oil) as well as C7-C18 carboxylic acids with ethoxylation of 1-10 moles of ethylene oxide. For this invention tall oil and the carboxylate Neodox 1-4 available from Shell Chemical Co. is especially preferred. We have also found that by the inclusion of the ethoxylated organic acid that that it not only improves product stability but enhances the stability of the concentrate when diluted in hard water so that no additional builder or chelate is necessary. Another key attribute was found with the unique use of alkaline salts like sodium hydroxide and potassium hydroxide. We have also found that by the use of these carboxylic acids combinations we obtained less viscous compositions which are much easier dispensed from venturi type dispenser than prior art compositions.
    The couplers are present in ready-to-use compositions of the invention such that the amount of the coupler is always less than or equal to the solvent blend used. This a departure from previous taught patents where said coupler are either equal to or as much as 3.0 times necessary to solubilize the solvents in water.
    Other optional surfactants that can be used in this invention are nonionics, in particular the Tergitols, such as Tergitol 15-S-9, which has been found to be useful in making formulations not containing ethoxylated carboxylates, however they are not the preferred surfactants. Tergitol is a trademark of Union Carbide Corporation for C8-C18 nonionic surfactants with 1-15 moles of ethylene oxide. Other anionic surfactants that have found utility are the well known hydrotropes like sodium xylene sulfonate as well as the following: dodecylbenzene sulfonic acid, sodium dodecylbenzene sulfonate, potassium dodecylbenzene sulfonate, triethanolamine dodecylbenzene sulfonate, morpholinium dodecylbenzene sulfonate, ammonium dodecylbenzene sulfonate, isopropylamine dodecylbenzene sulfonate, sodium tridecylbenzene sulfonate, sodium dinonylbenzene sulfonate, potassium didodecylbenzene sulfonate, dodecyl diphenyloxide disulfonic acid, sodium dodecyl diphenyloxide disulfonate, isopropylamine decyl diphenyloxide disulfonate, sodium hexadecyloxypoly (ethyleneoxy) (10) ethyl sulfonate, potassium octylphenoxypoly (ethyleneoxy) (9) ethyl sulfonate, sodium alpha C12-14 olefin sulfonate, sodium hexadecane-1 sulfonate, sodium ethyl oleate sulfonate, potassium octadecenylsuccinate, sodium oleate, potassium laurate, triethanolamine myristate, morpholinium tallate, potassium tallate, sodium lauryl sulfate, diethanolamine lauryl sulfate, sodium laureth (3) sulfate, ammonium laureth (2) sulfate, sodium nonylphenoxypoly (ethyleneoxy) (4) sulfate, sodium diisobutylsulfosuccinate, disodium laurylsulfosuccinate, tetrasodium N-laurylsulfosuccinimate, sodium mono decyloxypoly (ethyleneoxy) (4) phosphate, sodium di decyloxypoly (ethyleneoxy) (6) phosphate, and postassium mono/di-octylphenoxypoly (ethyleneoxy) (9) phosphate. These surfactants and hydrotropes were found to be especially useful in formulating other compositions that contained water soluble solvents like butyl Cellosolve.
    These compositions can also be thickened and used for various other applications especially for vertical surfaces and as an aerosol applications. Prior art describes the use of specific ingredients that are useful for those applications.
    In the methods of the invention, the compositions of the invention may be applied with a mop, poured onto the surface to be cleaned or stripped as well as dispensed from a suitable dispenser such as one of the venturi type (J-Fill dispenser). The compositions may also be applied by conventional floor maintenance machines, or they may be sprayed as an aerosol or non-aerosol upon the surface to be cleaned. Spraying can be accomplished by conventional mechanical spraying devices or by using an aerosol dispensing container with a sufficient amount of suitable aerosol propellant, for example, low boiling alkanes or mixtures thereof, such as a mixture of isobutane and propane..
    Further application of the compositions and methods of the invention will be understood with reference to the following Examples wherein all parts and percentages are by weight unless otherwise specified. These Examples are set forth to illustrate the invention and are not intended to limit the invention in any way.
    EXAMPLES
    The concentrated compositions shown in Table 1 above were diluted with water at the dilutions indicated in Table 2 to formulate the compositions of Examples 1-2. Table 2 also shows additional formulations and the various key compositions tested to arrive at the compositions of this invention. The compositions of comparative Examples A-C in Table 3 were formulated in accordance with the teaching of U.S. Patent No. 5,158,710; U.S. Patent No. 5,637,559 and Japanese Patent 9689885 and are provided in prior art Examples A-C.
    The composition of Examples 1-7 and Comparative Examples A-C were tested to determine their proficiency in removing 10 coats of a commercially available acrylic finishes from a composition vinyl tile strip, the finish available from SC Johnson Professional, Racine, WI under the trade designation of Signature. To clean previously stripped tiles 10 coats of finish was applied. After each coat a crayon marker was used to identify each coat. The Signature coated tiles were burnished (high speed burnisher) after 3, 6 and 10th coat prior to oven aging in order to enhance and duplicate actual aged coatings found in commerce. After all 10 coats were applied the tiles were aged in a oven at 52°C (125 F)for 100 hours to allow the coating to fully harden and thus simulate aged coating.
    The compositions of Examples 1-7 as well as Comparative Examples A-C were then tested via the use of a Gardner Scrubber by placing strips of tiles treated and identified onto the bed of the Scrubber. Each strip of tile was stripped with a red non-woven nylon pad which was attached to a pulley and is dragged over the tile to simulate the type of abrasion done in actual practice. To each strip of tile 15 mls of diluted concentrated stripper solutions were applied to the tile. Immediately after the solution was applied the Gardner Scrubber was started and number of coats removed versus cycles was recorded. In all Examples, the number of maximum cycles used was 100 cycles or less depending on complete removal.
    As a second method to determine stability of both the concentrate as well as dilution, comparative as well as compositions were tested via two methods. The first method for composition stability was to make up the composition and subject it to both 4°C (40 F) and 52°C (125 F) in a refrigerator or oven for at least 3 days The results are also included. A second test which determined the stability of the diluted product was done by diluting the concentrates in synthetic 300 ppm hard water (as CaCO3). The results from this test is also indicated in the Tables. These tests are used by those skilled in the art of developing compositions and are readily accepted as an indication of the overall microemulsion properties and efficiency of the surfactants/solvents used.
    The third test run was viscosity at 7°C (44 F) which gives a good indication of the rheology of the composition and is crucial in dispensing from venturi type dispenser (J-Fill), The lower the viscosity the more accurate the dilutions which are critical in performance. Viscosities greater than 50 cps can be used but viscosities less than 40 cps are preferred.
    Ingredient Ex. 1 Ex.2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7
    Monoethanol Amine 35 17 35.0 35 35 35 35
    Benzyl Alcohol 27.5 27.5 27.5 13.75 41.25
    Hexyl Cellosolve 27.5 27.5 27.5 41.25 13.75 27.5 27.5
    1-Butoxy Propanol 27.5
    Ethylene Glycol Phenyl Ether 27.5
    Tall Oil Fatty Acid 5.0 5.0 10.0 10.0 5.0 5.0
    Tergitol 15-S-9 5.0
    Neodox 1-4 5.0 10.0
    Neodox 45-6 5.0 5.0
    Potassium Hydroxide 18.0
    No. of coats Signature Removed
    Dilution @ 1:15 9 10 8
       @ 1:25 8 8 6
    Dilution Stability-Conc. pass* pass pass sep* sep sep sep
       @1:15(hard water) pass pass pass sep sep
       @1:25(hard water) pass pass pass
       @1:256(hard water) pass pass pass
    Viscosity @ 7°C (44 F)(cps) 44.8 76.8 44.8
    PRIOR ART EXAMPLES Example A - 3M Formulation
    Ingredient %/Wt
    Monoethanolamine 33.9
    Benzyl Alcohol 39.9
    n-Octanoic Acid 25.0
    FC-135 0.20
    Dye 0.50
    Chelating Agent 0.50
    Example B - Butchers Full Impact
    Ingredient %/Wt
    Monoethanolamine 23.2
    Benzyl Alcohol 47.9
    Dipropylene Glycol n-Butyl Ether 13.5 (water soluble solvent)
    Tall Oil FA Salt (Amine) 15.4
    Example C - Japan Power - Go
    Ingredient %/Wt
    Monoethanolamine 18.0
    N-(,B Aminoethyl) Ethanolamine 15.0
    Benzyl Alcohol 35.0
    Tall Oil Fatty Acid 5.0
    Fluoroalcohol Phosphate and Eto 0.1
    Quatermonium Salt
    Perfluoro Alky Phosphate (15%) 0.6
    Fluorinated Acrylic Ester
    Copolymer (20%) 0.1
    Water 26.2
    Comparative Examples A-C
    3M Formulation A
    Butchers Full Impact B
    Japan Power-Go C
    No. of coats Signature Removed
    Dilution @1:15 7 8 7
       @1:25 6 7 3
    Dilution Stability-Conc pass pass pass
       @1:15(hard water) pcpt pcpt pcpt
       @1:25(hard water) pcpt pcpt pcpt
       @1:256(hard water) pcpt pcpt pcpt
    Viscosity @ 7°C (44F)(cps) 102.4 25.6 27.0
    Pcpt-refers to substantial precipitation when concentrate is diluted.
    These Examples A-C as well as Examples 1-7 illustrate the importance of the ethoxylated anionic surfactant coupler if it is to be diluted and still act as an effective stripper.
    While certain alkyl and aryl ethers as well as alkyl alcohols have been indicated for use with the phenyl substituted alkyl alcohols of this invention, other alkyl and aryl ethers as well as alkyl and aromatic alcohols can be employed which are described as follows according to their water solubility.
    WATER SOLUBLE: >6.0 Wt. Percent soluble in water
    Ethylene Glycol Monobutyl Ether
    Propylene Glycol methyl ether
    2-Tertiary Butoxy Ethanol
    Dipropylene Glycol Methyl Ether
    Tripropylene Glycol Methyl Ether
    Propylene Glycol n-Propyl Ether
    Dipropylene Glycol n-Propyl Ether
    Diethylene Glycol n-Butyl Ether
    Butoxytriglycol
    Triethylene Glycol n-Butyl Ether
    Diethylene Glycol Methyl Ether
    Triethylene Glycol Methyl Ether
    Ethylene Glycol Monopropyl Ether
    Diethylene Glycol Monomethyl Ether
    Methoxytriglycol
    Ethoxytriglycol
    SPARINGLY WATER SOLUBLE: <6.0 Wt. Percent soluble in water
    1-phenoxy-2-propanol
    Propylene Glycol n-Butyl Ether
    Dipropylene Glycol n-Butyl Ether
    Tripropylene Glycol n-Butyl Ether
    Propylene Glycol Phenyl Ether
    2-Octanol
    Cyclohexanol
    iso-octanol
    Texanol (Eastman)
    n-decanol
    Diethylene Glycol mono hexyl Ether
    2-Ethyl Hexanol
    INDUSTRIAL APPLICABILITY
    The compositions of this invention are useful in stripping and removing coatings such as floor finishes as well as the cleaning of such surfaces. They can be diluted with water and still provide stripping and cleaning properties.

    Claims (9)

    1. A composition suitable for stripping coatings from a surface the composition comprising:
      a. 1-55% by weight of a solvent mixture composed of a phenyl substituted alkyl alcohol and an equal amount by weight of an alkyl or aryl glycol ether or an alkyl or aromatic alcohol, said solvent mixture effective in removing at least 20 % of a standard acrylic floor sealer/finish from a composition vinyl tile in fewer than 2.5 minutes;
      b. a coupler composed of a salt formed from a water soluble organic amine and an acid comprising at least one C7-C18 ethoxylated anionic surfactant, said coupler and said solvent mixture present in weight ratio of solvent mixture present in a weight ratio of 1:1.2 to 1:2.0 wherein the amount of the coupler is at least 2 times the amount necessary to completely solubilize the solvent mixture; and
      c. optionally water.
    2. Composition in accordance with Claim 1 wherein the water-soluble organic amine is monoethanolamine or a combination of monoethanolamine and potassium hydroxide.
    3. Composition in accordance with Claim 1 wherein the acid is a C9-C11 ethoxylated anionic surfactant.
    4. Composition in accordance with Claim 2 wherein the acid has 4 moles of ethoxylation.
    5. Composition in accordance with Claim 1 wherein the phenyl substituted alkyl alcohol is benzyl alcohol.
    6. Composition in accordance with Claim 1 wherein the alkyl glycol ether is ethylene glycol monohexyl ether.
    7. The Composition in accordance with Claim 1 wherein the coupler further includes tall oil.
    8. Composition in accordance with Claim 1 wherein the solvent mixture has a water solubility of at least 0.1 weight percent.
    9. A method of removing a coating from a surface comprising:
      applying to the coating the composition of Claim 1; and
      allowing the composition to contact the coating for a time sufficient to at least partially remove the coating.
    EP99954639A 1998-10-01 1999-09-22 Concentrated stripper composition and method Expired - Lifetime EP1119591B1 (en)

    Applications Claiming Priority (3)

    Application Number Priority Date Filing Date Title
    US09/164,748 US5977042A (en) 1998-10-01 1998-10-01 Concentrated stripper composition and method
    US164748 1998-10-01
    PCT/US1999/021764 WO2000020518A1 (en) 1998-10-01 1999-09-22 Concentrated stripper composition and method

    Publications (2)

    Publication Number Publication Date
    EP1119591A1 EP1119591A1 (en) 2001-08-01
    EP1119591B1 true EP1119591B1 (en) 2003-11-19

    Family

    ID=22595930

    Family Applications (1)

    Application Number Title Priority Date Filing Date
    EP99954639A Expired - Lifetime EP1119591B1 (en) 1998-10-01 1999-09-22 Concentrated stripper composition and method

    Country Status (13)

    Country Link
    US (1) US5977042A (en)
    EP (1) EP1119591B1 (en)
    JP (1) JP4606585B2 (en)
    KR (1) KR100625147B1 (en)
    CN (1) CN1247715C (en)
    AT (1) ATE254650T1 (en)
    AU (1) AU756614B2 (en)
    BR (1) BR9914188B1 (en)
    CA (1) CA2345692C (en)
    DE (1) DE69912976T2 (en)
    ES (1) ES2211190T3 (en)
    NZ (1) NZ510701A (en)
    WO (1) WO2000020518A1 (en)

    Cited By (1)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    US11851637B2 (en) * 2013-08-23 2023-12-26 Ecolab Usa Inc. Adhesive remover compositions and methods of use

    Families Citing this family (44)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    US6197844B1 (en) * 1996-09-13 2001-03-06 3M Innovative Properties Company Floor finish compositions
    US6564814B2 (en) * 1997-05-23 2003-05-20 Shelba F. Bowsman Engine decarbonizing system
    US6200940B1 (en) * 1999-07-19 2001-03-13 Napier International Technologies, Inc. Paint stripper compositions
    US6303552B1 (en) * 1999-08-04 2001-10-16 Napier International Technologies, Inc. Aerosol paint stripper compositions
    US6583101B1 (en) * 1999-08-25 2003-06-24 Ecolab Inc. Aqueous organic dispersions suitable for removing organic films and soils
    AU764440B2 (en) * 1999-08-25 2003-08-21 Ecolab Inc. Method for removing an ultraviolet light cured floor finish, removable ultraviolet light curable floor finish and strippable finished floor
    US6583097B2 (en) 2000-01-21 2003-06-24 Mary E. McDonald Universal cleaner that cleans tough oil, grease and rubber grime and that is compatible with many surfaces including plastics
    WO2001082694A1 (en) 2000-04-28 2001-11-08 Ecolab Inc. Antimicrobial composition
    US6544942B1 (en) * 2000-04-28 2003-04-08 Ecolab Inc. Phase-separating solvent composition
    US6593283B2 (en) * 2000-04-28 2003-07-15 Ecolab Inc. Antimicrobial composition
    AU5377801A (en) * 2000-04-28 2001-11-12 Ecolab Inc Strippable laminate finish
    US6800353B1 (en) 2000-09-08 2004-10-05 Ecolab Inc. Scratch-resistant strippable finish
    US20030125226A1 (en) * 2000-11-28 2003-07-03 Lewis Paul F. Anti-slip floor coating remover composition
    US7482316B2 (en) * 2001-01-04 2009-01-27 Henkel Kommanditgesellschaft Auf Aktien Water-based flushing solution for paints and other coatings
    US6558795B2 (en) 2001-04-20 2003-05-06 Ecolab Inc. Strippable coating system
    KR100779037B1 (en) * 2001-09-26 2007-11-27 주식회사 동진쎄미켐 A color resist remover composition for tft-lcd preparation
    WO2003052004A1 (en) * 2001-12-14 2003-06-26 Aero-Chem, Llc Cyclic ether based paint remover
    US20030220213A1 (en) * 2002-05-24 2003-11-27 Bober Andrew M. Color changing floor finish stripper
    US7008911B2 (en) * 2002-09-06 2006-03-07 Ecolab, Inc. Non-surfactant solubilizing agent
    US7071155B2 (en) * 2002-10-02 2006-07-04 Eoclab, Inc. Non-polymer thickening agent and cleaning composition
    US7211551B2 (en) * 2002-10-21 2007-05-01 Mcdonald Mary E Universal cleaner that cleans tough oil, grease and rubber grime and that is compatible with many surfaces including plastics
    KR100805014B1 (en) * 2003-08-27 2008-02-20 가켄 테크 가부시키가이샤 Cleaning agent for removing solder flux and method for cleaning solder flux
    DE10357389B4 (en) * 2003-12-07 2005-12-15 Benda, Jürgen Michael Process for cleaning soapstone
    JP4610920B2 (en) * 2004-03-30 2011-01-12 スイショウ油化工業株式会社 Release agent composition and method for producing the same
    SE528010C2 (en) * 2004-12-30 2006-08-01 Stripp Chemicals Ab Means for removing paint, varnish glue, rubber, plastic or the like from objects and use of said agents
    CN1743965B (en) * 2005-09-30 2010-05-05 廊坊开发区普瑞特科工贸有限公司 Environmental-protection type regenerative PS plate ink and photoresists stripping agent and its preparing method
    US20070087952A1 (en) * 2005-10-18 2007-04-19 Ecolab Inc. Floor stripper/cleaner containing aliphatic acid-organic base pair
    US7674760B2 (en) * 2005-10-18 2010-03-09 Ecolab Inc. Floor stripper/cleaner containing organic acid-base pair
    US20090131296A1 (en) * 2007-11-21 2009-05-21 Ecolab Inc. Floor Stripper For Chemically-Resistant Crosslinked Floor Finishes
    AU2007361442B2 (en) * 2007-11-21 2013-01-31 Ecolab Inc. Floor stripper for chemically-resistant crosslinked floor finishes
    WO2010146544A2 (en) * 2009-06-15 2010-12-23 Ecolab Usa Inc. High alkaline solvent-based cleaners, cleaning systems and methods of use for cleaning zero trans fat soils
    US8394751B2 (en) * 2010-01-29 2013-03-12 W. M. Barr & Company Organic residue remover composition
    WO2011146832A2 (en) * 2010-05-20 2011-11-24 Diversey, Inc. Stripping compositions and methods of making and using the same
    ES2663201T3 (en) 2011-05-20 2018-04-11 Ecolab Usa Inc. Non-corrosive oven degreasing concentrate
    CN103157621A (en) * 2011-12-13 2013-06-19 贵州黎阳航空动力有限公司 Chemical method for clearing sealant and solution prepared by using chemical method
    US9309485B2 (en) 2013-06-26 2016-04-12 Ecolab USA, Inc. Use of nonionics as rheology modifiers in liquid cleaning solutions
    JP6310727B2 (en) * 2013-11-29 2018-04-11 株式会社ニイタカ Floor polish release agent and floor polish release method
    US10260026B2 (en) * 2014-10-21 2019-04-16 Dow Global Technologies Llc Method for dissolution of polymerized soil
    TWI608311B (en) * 2016-03-25 2017-12-11 達興材料股份有限公司 A photoresist stripper composition and a photolithography process for manufacturing a electronic device utilizing the same
    KR102077953B1 (en) 2016-05-10 2020-02-14 아토테크더치랜드게엠베하 Methods of Stripping Organic Coatings from Non-Aqueous Stripping Compositions and Substrates
    JP6975969B2 (en) * 2017-11-13 2021-12-01 シーバイエス株式会社 Cleaning agent composition for crosslinked coating film and floor management method
    WO2019108990A1 (en) 2017-12-01 2019-06-06 Ecolab Usa Inc. Cleaning compositions and methods for removing baked on grease from fryers and other hot surfaces
    JP7280279B2 (en) * 2018-03-20 2023-05-23 ローム アンド ハース カンパニー Neutralizer composition
    US20230058960A1 (en) * 2020-01-23 2023-02-23 Reckitt & Colman (Overseas) Hygiene Home Limited Oven cleaning compositions and methods of making and using same

    Family Cites Families (12)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    US4414128A (en) * 1981-06-08 1983-11-08 The Procter & Gamble Company Liquid detergent compositions
    US4749509A (en) * 1986-11-24 1988-06-07 The Proctor & Gamble Company Aqueous detergent compositions containing diethyleneglycol monohexyl ether solvent
    US5158710A (en) * 1989-06-29 1992-10-27 Buckeye International, Inc. Aqueous cleaner/degreaser microemulsion compositions
    US5080831A (en) * 1989-06-29 1992-01-14 Buckeye International, Inc. Aqueous cleaner/degreaser compositions
    US5080822A (en) * 1990-04-10 1992-01-14 Buckeye International, Inc. Aqueous degreaser compositions containing an organic solvent and a solubilizing coupler
    US5454985A (en) * 1992-11-06 1995-10-03 Gage Products Company Paint stripping composition
    DE69412080T2 (en) * 1993-03-30 1999-04-08 Minnesota Mining & Mfg IMPROVED FLOOR SEALING COMPOSITION AND METHOD
    US5543073A (en) * 1993-04-14 1996-08-06 Colgate-Palmolive Company Microemulsion cleaning composition
    US5636559A (en) * 1993-10-07 1997-06-10 Smithwick, Jr.; James M. Elastomeric scrap ejector for a cutting die
    US5411678A (en) * 1994-02-07 1995-05-02 Mcgean-Rohco, Inc. Paint stripper
    JPH0889885A (en) * 1994-09-20 1996-04-09 Bridgestone Corp Transfer coating method for roller
    JP4013998B2 (en) * 1996-03-07 2007-11-28 ジョンソンディバーシー株式会社 Release agent for water-based polymer type floor polish

    Cited By (1)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    US11851637B2 (en) * 2013-08-23 2023-12-26 Ecolab Usa Inc. Adhesive remover compositions and methods of use

    Also Published As

    Publication number Publication date
    BR9914188A (en) 2001-08-14
    NZ510701A (en) 2002-05-31
    CA2345692A1 (en) 2000-04-13
    CN1320143A (en) 2001-10-31
    EP1119591A1 (en) 2001-08-01
    BR9914188B1 (en) 2008-11-18
    CA2345692C (en) 2005-01-18
    JP4606585B2 (en) 2011-01-05
    WO2000020518A1 (en) 2000-04-13
    KR100625147B1 (en) 2006-09-20
    AU756614B2 (en) 2003-01-16
    ES2211190T3 (en) 2004-07-01
    DE69912976T2 (en) 2004-09-02
    ATE254650T1 (en) 2003-12-15
    DE69912976D1 (en) 2003-12-24
    KR20010073199A (en) 2001-07-31
    JP2002526629A (en) 2002-08-20
    US5977042A (en) 1999-11-02
    AU1094100A (en) 2000-04-26
    CN1247715C (en) 2006-03-29

    Similar Documents

    Publication Publication Date Title
    EP1119591B1 (en) Concentrated stripper composition and method
    EP0692004B1 (en) Improved floor stripping composition and method
    US4983317A (en) All purpose cleaner concentrate composition
    AU668201B2 (en) Thickened acid microemulsion composition
    EP0479908B1 (en) Improved aqueous cleaner/degreaser compositions
    JPH09509438A (en) Dual-purpose cleaning composition for paint and waxed surfaces
    WO1994023003A1 (en) Cleaning compositions and methods of use
    WO1997009407A1 (en) Fully diluted hard surface cleaners containing small amounts of certain acids
    EP0900270A1 (en) Thickened acid composition
    US6465411B2 (en) Pine oil cleaning composition
    JP2020519720A (en) Compositions and methods for floor cleaning or repair
    JP2608327B2 (en) Bathroom cleaning composition
    US5837667A (en) Environmentally safe detergent composition and method of use
    MXPA01003342A (en) Concentrated stripper composition and method
    CN1052028C (en) Improved floor stripping composition and method
    JPH09241686A (en) Industrial degreasing cleaner
    CN117025311A (en) Deep cleaning agent for station building counter facilities
    CA2504646C (en) Cleaning composition and method of use
    JP2935194B2 (en) Aerosol foaming detergent composition
    CA2190594C (en) Cleaning compositions
    JP2003206498A (en) Cleanser composition

    Legal Events

    Date Code Title Description
    PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

    Free format text: ORIGINAL CODE: 0009012

    17P Request for examination filed

    Effective date: 20010411

    AK Designated contracting states

    Kind code of ref document: A1

    Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

    AX Request for extension of the european patent

    Free format text: AL;LT;LV;MK;RO;SI

    GRAG Despatch of communication of intention to grant

    Free format text: ORIGINAL CODE: EPIDOS AGRA

    17Q First examination report despatched

    Effective date: 20011210

    GRAG Despatch of communication of intention to grant

    Free format text: ORIGINAL CODE: EPIDOS AGRA

    GRAH Despatch of communication of intention to grant a patent

    Free format text: ORIGINAL CODE: EPIDOS IGRA

    RAP1 Party data changed (applicant data changed or rights of an application transferred)

    Owner name: JOHNSONDIVERSEY, INC.

    GRAG Despatch of communication of intention to grant

    Free format text: ORIGINAL CODE: EPIDOS AGRA

    GRAH Despatch of communication of intention to grant a patent

    Free format text: ORIGINAL CODE: EPIDOS IGRA

    GRAH Despatch of communication of intention to grant a patent

    Free format text: ORIGINAL CODE: EPIDOS IGRA

    GRAA (expected) grant

    Free format text: ORIGINAL CODE: 0009210

    AK Designated contracting states

    Kind code of ref document: B1

    Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: FI

    Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

    Effective date: 20031119

    Ref country code: CY

    Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

    Effective date: 20031119

    Ref country code: AT

    Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

    Effective date: 20031119

    REG Reference to a national code

    Ref country code: GB

    Ref legal event code: FG4D

    REG Reference to a national code

    Ref country code: CH

    Ref legal event code: EP

    REF Corresponds to:

    Ref document number: 69912976

    Country of ref document: DE

    Date of ref document: 20031224

    Kind code of ref document: P

    REG Reference to a national code

    Ref country code: IE

    Ref legal event code: FG4D

    REG Reference to a national code

    Ref country code: CH

    Ref legal event code: NV

    Representative=s name: E. BLUM & CO. PATENTANWAELTE

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: SE

    Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

    Effective date: 20040219

    Ref country code: GR

    Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

    Effective date: 20040219

    Ref country code: DK

    Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

    Effective date: 20040219

    LTIE Lt: invalidation of european patent or patent extension

    Effective date: 20031119

    REG Reference to a national code

    Ref country code: ES

    Ref legal event code: FG2A

    Ref document number: 2211190

    Country of ref document: ES

    Kind code of ref document: T3

    ET Fr: translation filed
    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: LU

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20040922

    PLBE No opposition filed within time limit

    Free format text: ORIGINAL CODE: 0009261

    STAA Information on the status of an ep patent application or granted ep patent

    Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: MC

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20040930

    26N No opposition filed

    Effective date: 20040820

    REG Reference to a national code

    Ref country code: CH

    Ref legal event code: PFA

    Owner name: JOHNSONDIVERSEY, INC.

    Free format text: JOHNSONDIVERSEY, INC.#8310 16TH STREET#STURTEVANT, WISCONSIN 53177-0902 (US) -TRANSFER TO- JOHNSONDIVERSEY, INC.#8310 16TH STREET#STURTEVANT, WISCONSIN 53177-0902 (US)

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: PT

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20040419

    PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

    Ref country code: IE

    Payment date: 20080925

    Year of fee payment: 10

    REG Reference to a national code

    Ref country code: IE

    Ref legal event code: MM4A

    REG Reference to a national code

    Ref country code: CH

    Ref legal event code: PFA

    Owner name: DIVERSEY, INC.

    Free format text: JOHNSONDIVERSEY, INC.#8310 16TH STREET#STURTEVANT, WISCONSIN 53177-0902 (US) -TRANSFER TO- DIVERSEY, INC.#8310 16TH STREET - M/S 509#STURTEVANT, WI 53177-0902 (US)

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: IE

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20090922

    REG Reference to a national code

    Ref country code: NL

    Ref legal event code: TD

    Effective date: 20101013

    REG Reference to a national code

    Ref country code: FR

    Ref legal event code: CD

    REG Reference to a national code

    Ref country code: ES

    Ref legal event code: PC2A

    Owner name: DIVERSEY, INC.

    Effective date: 20110429

    REG Reference to a national code

    Ref country code: NL

    Ref legal event code: PLEX

    Effective date: 20120724

    PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

    Ref country code: DE

    Payment date: 20130927

    Year of fee payment: 15

    Ref country code: ES

    Payment date: 20130926

    Year of fee payment: 15

    Ref country code: NL

    Payment date: 20130926

    Year of fee payment: 15

    PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

    Ref country code: GB

    Payment date: 20130927

    Year of fee payment: 15

    Ref country code: FR

    Payment date: 20130919

    Year of fee payment: 15

    PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

    Ref country code: IT

    Payment date: 20130925

    Year of fee payment: 15

    PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

    Ref country code: BE

    Payment date: 20130927

    Year of fee payment: 15

    Ref country code: CH

    Payment date: 20130927

    Year of fee payment: 15

    REG Reference to a national code

    Ref country code: DE

    Ref legal event code: R119

    Ref document number: 69912976

    Country of ref document: DE

    REG Reference to a national code

    Ref country code: CH

    Ref legal event code: PL

    GBPC Gb: european patent ceased through non-payment of renewal fee

    Effective date: 20140922

    REG Reference to a national code

    Ref country code: FR

    Ref legal event code: ST

    Effective date: 20150529

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: BE

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140930

    Ref country code: NL

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20150401

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: LI

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140930

    Ref country code: DE

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20150401

    Ref country code: CH

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140930

    Ref country code: GB

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140922

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: FR

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140930

    Ref country code: IT

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140922

    REG Reference to a national code

    Ref country code: ES

    Ref legal event code: FD2A

    Effective date: 20151026

    PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

    Ref country code: ES

    Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

    Effective date: 20140923